WO2006095127A1 - A fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement - Google Patents

A fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement Download PDF

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Publication number
WO2006095127A1
WO2006095127A1 PCT/GB2006/000487 GB2006000487W WO2006095127A1 WO 2006095127 A1 WO2006095127 A1 WO 2006095127A1 GB 2006000487 W GB2006000487 W GB 2006000487W WO 2006095127 A1 WO2006095127 A1 WO 2006095127A1
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WIPO (PCT)
Prior art keywords
fuel
supply
partial oxidation
reactor
cell arrangement
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PCT/GB2006/000487
Other languages
French (fr)
Inventor
Gary John Saunders
Fabio Cerutti
Original Assignee
Rolls-Royce Fuel Cell Systems Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Rolls-Royce Fuel Cell Systems Limited filed Critical Rolls-Royce Fuel Cell Systems Limited
Priority to EP06709724.6A priority Critical patent/EP1864350B1/en
Priority to AU2006221822A priority patent/AU2006221822B2/en
Priority to JP2008504822A priority patent/JP5063584B2/en
Priority to US11/884,229 priority patent/US8147571B2/en
Priority to KR1020077019109A priority patent/KR101363337B1/en
Priority to DK06709724.6T priority patent/DK1864350T3/en
Priority to ES06709724.6T priority patent/ES2476997T3/en
Priority to CA002596919A priority patent/CA2596919A1/en
Publication of WO2006095127A1 publication Critical patent/WO2006095127A1/en
Priority to US13/292,847 priority patent/US8470482B2/en
Priority to US13/872,710 priority patent/US8568494B2/en

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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0662Treatment of gaseous reactants or gaseous residues, e.g. cleaning
    • H01M8/0675Removal of sulfur
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    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/22Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of gaseous or liquid organic compounds
    • C01B3/24Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of gaseous or liquid organic compounds of hydrocarbons
    • C01B3/26Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of gaseous or liquid organic compounds of hydrocarbons using catalysts
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    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/382Multi-step processes
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    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/386Catalytic partial combustion
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/04Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0606Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
    • H01M8/0612Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0662Treatment of gaseous reactants or gaseous residues, e.g. cleaning
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    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02Processes for making hydrogen or synthesis gas
    • C01B2203/0205Processes for making hydrogen or synthesis gas containing a reforming step
    • C01B2203/0227Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step
    • C01B2203/0233Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being a steam reforming step
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02Processes for making hydrogen or synthesis gas
    • C01B2203/0205Processes for making hydrogen or synthesis gas containing a reforming step
    • C01B2203/0227Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step
    • C01B2203/0238Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being a carbon dioxide reforming step
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02Processes for making hydrogen or synthesis gas
    • C01B2203/025Processes for making hydrogen or synthesis gas containing a partial oxidation step
    • C01B2203/0261Processes for making hydrogen or synthesis gas containing a partial oxidation step containing a catalytic partial oxidation step [CPO]
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/06Integration with other chemical processes
    • C01B2203/066Integration with other chemical processes with fuel cells
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08Methods of heating or cooling
    • C01B2203/0805Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/0811Methods of heating the process for making hydrogen or synthesis gas by combustion of fuel
    • C01B2203/0827Methods of heating the process for making hydrogen or synthesis gas by combustion of fuel at least part of the fuel being a recycle stream
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/10Catalysts for performing the hydrogen forming reactions
    • C01B2203/1041Composition of the catalyst
    • C01B2203/1047Group VIII metal catalysts
    • C01B2203/1052Nickel or cobalt catalysts
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/10Catalysts for performing the hydrogen forming reactions
    • C01B2203/1041Composition of the catalyst
    • C01B2203/1047Group VIII metal catalysts
    • C01B2203/1052Nickel or cobalt catalysts
    • C01B2203/1058Nickel catalysts
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1205Composition of the feed
    • C01B2203/1211Organic compounds or organic mixtures used in the process for making hydrogen or synthesis gas
    • C01B2203/1235Hydrocarbons
    • C01B2203/1241Natural gas or methane
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1258Pre-treatment of the feed
    • C01B2203/1264Catalytic pre-treatment of the feed
    • C01B2203/127Catalytic desulfurisation
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/14Details of the flowsheet
    • C01B2203/142At least two reforming, decomposition or partial oxidation steps in series
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/14Details of the flowsheet
    • C01B2203/148Details of the flowsheet involving a recycle stream to the feed of the process for making hydrogen or synthesis gas
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/16Controlling the process
    • C01B2203/1604Starting up the process
    • CCHEMISTRY; METALLURGY
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    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/16Controlling the process
    • C01B2203/1609Shutting down the process
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/141Feedstock
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Definitions

  • the present invention relates to a fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement.
  • the pre-reformer comprises a catalyst suitable for low temperature steam reforming of the hydrocarbon fuel and a catalyst for partial oxidation reforming of the hydrocarbon fuel.
  • the pre-reformer also comprises a catalyst suitable for hydrodesulphurisation of the hydrocarbon fuel.
  • a problem with this arrangement is that at low electrical load conditions, or at open circuit conditions, of the fuel cell arrangement, the fuel cells do not generate steam for the low temperature steam reforming reaction.
  • a further problem with this arrangement is that the hydrodesulphurisation of the hydrocarbon fuel is dependent on the rate of anode off gas, hydrogen, recirculation and this is dependent upon the operating conditions of the fuel cell arrangement.
  • the present invention seeks to provide a novel fuel processor for a fuel cell arrangement and a novel method of operating a fuel processor for a fuel cell arrangement to at least reduce or overcome the above- mentioned problem.
  • the present invention provides a fuel processor for a fuel cell arrangement comprising means to supply safe gas to the fuel cell arrangement in a first mode of operation, means to supply synthesis gas to the fuel cell arrangement in a second mode of operation and means to supply processed hydrocarbon fuel to the fuel cell arrangement in a third mode of operation.
  • the fuel processor comprises a desulphurisation reactor, a catalytic partial oxidation reactor, a combustor and a pre-reformer, means to supply a hydrocarbon fuel to the desulphurisation reactor, means to supply air to the catalytic partial oxidation reactor, means to supply air to the combustor, the desulphurisation reactor being arranged to supply desulphurised hydrocarbon fuel to the catalytic partial oxidation reactor, the combustor and to the pre-reformer, the combustor being arranged to supply oxygen depleted air and steam to the pre-reformer, the catalytic partial oxidation reactor being arranged to supply hydrogen to the desulphurisation reactor, the catalytic partial oxidation reactor being arranged to supply the pre-reformer, the pre-reformer being arranged to supply product gases to the fuel cell arrangement .
  • the fuel processor comprises a desulphurisation reactor, a catalytic partial oxidation reactor, a combustor and a pre-reformer, means to supply a hydrocarbon fuel to the desulphurisation reactor, means to supply hydrocarbon fuel to the catalytic partial oxidation reactor, means to supply air to the catalytic partial oxidation reactor, means to supply air to the combustor, the desulphurisation reactor being arranged to supply desulphurised hydrocarbon fuel to the combustor and to the pre-reformer, the combustor being arranged to supply oxygen depleted air and steam to the pre-reformer, the catalytic partial oxidation reactor being arranged to supply hydrogen to the desulphurisation reactor, the pre-reformer being arranged to supply product gases to the fuel cell arrangement .
  • the present invention also provides a method of operating a fuel processor for a fuel cell arrangement comprising
  • (c) supplying processed hydrocarbon fuel to the fuel cell arrangement in a third mode of operation.
  • the first mode is start up and/or shut down conditions of the fuel cell arrangement.
  • the second mode is hot idle and/or part load conditions of the fuel cell arrangement.
  • the third mode is normal conditions of the fuel cell arrangement.
  • the first mode of operation comprises desulphurising a hydrocarbon fuel, carrying out catalytic partial oxidation on the desulphurised hydrocarbon fuel to produce a synthesis gas, burning the desulphurised hydrocarbon fuel to produce oxygen depleted gas and mixing the synthesis gas with the oxygen depleted gas to produce safe gas.
  • the second mode of operation comprises desulphurising a hydrocarbon fuel, carrying out catalytic partial oxidation on the desulphurised hydrocarbon fuel to produce a synthesis gas.
  • the third mode of operation comprises desulphurising a hydrocarbon fuel, carrying out catalytic partial oxidation on the desulphurised hydrocarbon fuel to produce a synthesis gas, mixing the synthesis gas with desulphurised hydrocarbon fuel and pre-reforming the desulphurised hydrocarbon fuel to produce the processed hydrocarbon fuel.
  • the desulphurising comprises mixing synthesis gas and the hydrocarbon fuel to react hydrogen in the synthesis gas with sulphur compounds in the hydrocarbon fuel to form hydrogen sulphide.
  • the desulphurising comprises adsorbing the hydrogen sulphide.
  • the pre-reforming of the desulphurised hydrocarbon fuel comprises hydrogenolysis .
  • the safe gas comprises low partial pressures of hydrogen and carbon monoxide.
  • the safe gas contains approximately 5vol% flammable gases and the remainder is non-flammable gases.
  • the synthesis gas comprises high partial pressures of hydrogen and carbon monoxide.
  • the synthesis gas contains approximately 33 vol% hydrogen and 17 vol% carbon monoxide and the remainder is non-flammable gases.
  • Figure 1 shows a fuel processor according to the present invention.
  • Figure 2 shows an alternative fuel processor according to the present invention.
  • a fuel processor 10 for a fuel cell arrangement comprises a hydrodesulphurisation reactor 12, a catalytic partial oxidation reactor 14, a combustor 16 and a pre- reformer 18.
  • the hydrodesulphurisation reactor 12 is connected to the pre-reformer 18 via a pipe 32 and a valve 34.
  • the hydrodesulphurisation reactor 12 is connected to the catalytic partial oxidation reactor 14 via pipes 32 and 36.
  • the hydrodesulphurisation reactor 12 is also connected to the combustor 16 via pipes 32 and 38 and a valve 40.
  • the combustor 16 is connected to the pre-reformer 18 via pipes 42 and 32.
  • the catalytic partial oxidation reactor 14 is connected to the pre-reformer 18 via pipes 44 and 32.
  • the catalytic partial oxidation reactor 14 is connected to the hydrodesulphurisation reactor 12 via a pipe 46 and a recirculating means 54, the recirculating means may comprise an ejector, a fan, a pump etc.
  • the pre-reformer 18 is connected to supply product gases to the fuel cell arrangement or, a further device, via a pipe 48.
  • the means 20 to supply hydrocarbon fuel for example is a supply of natural gas.
  • the means 24 to supply air may be an air compressor, or pump, or an air source within the pressure vessel of the fuel cell arrangement.
  • valve 50 may be provided in pipe 26 and a valve 52 may be provided in pipe 36 in order to isolate the catalytic partial oxidation reactor 14 if necessary.
  • the fuel processor 10 is arranged to perform a number of functions. Firstly the fuel processor 10 is arranged to remove sulphur from the hydrocarbon fuel such that the concentration of sulphur can be tolerated by the catalysts and components of the fuel cells. Secondly the fuel processor 10 is arranged to convert the hydrocarbon into a gas mixture, which contains low partial pressures of hydrogen and carbon monoxide, also known as "safe gas”. The "safe gas” contains approximately 5vol% flammable gases and the remainder is non-flammable gases. Thirdly the fuel processor 10 is arranged to convert hydrocarbon fuel into a gas mixture, which contains high partial pressures of hydrogen and carbon monoxide, also known as "synthesis gas or syngas".
  • the "synthesis gas” contains approximately 33 vol% hydrogen and 17 vol% carbon monoxide and the remainder is non-flammable gases.
  • the fuel processor 10 is arranged to remove higher hydrocarbons, including ethane, ethene, propane, propene, butane, butene, etc by converting them into methane.
  • the catalytic partial oxidation reactor 14 is arranged to continuously provide hydrogen to the hydrodesulphurisation reactor 12.
  • the catalytic partial oxidation reactor 14 is arranged to provide hydrogen to the pre-reformer 18 during start up of the fuel cell arrangement. During start up of the fuel cell arrangement the hydrogen and carbon monoxide is combined with an excess of non-flammable gases to form the safe gas.
  • the catalytic partial oxidation reactor 14 is also arranged to provide hydrogen and carbon monoxide to the fuel cell arrangement during hot idle conditions and part load conditions of the fuel cell arrangement. During hot idle conditions and part load conditions of the fuel cell arrangement the hydrogen and carbon monoxide is combined with non-flammable gases to form the synthesis gas.
  • the combustor 16 is arranged to provide oxygen depleted air and steam to the pre-reformer 18 during start up and shut down of the fuel cell arrangement.
  • the combustor 16 may also provide heat to the other reactors during start up such that those reactors reach operational temperature as quickly as possible.
  • the pre-reformer 18 is arranged to provide pre- reforming of higher hydrocarbons, those with more than one carbon atom, to prevent thermal cracking of the higher hydrocarbons in the fuel cell arrangement.
  • the pre- reforming of the higher hydrocarbons is by hydrogenolysis, steam reforming, carbon dioxide reforming, catalytic partial oxidation or any combination of these reactions.
  • the dominant reaction is hydrogenolysis.
  • hydrocarbon fuel for example natural gas
  • hydrocarbon fuel for example natural gas
  • the catalytic partial oxidation reactor 14 is supplied with the hydrocarbon fuel, natural gas, from the hydrodesulphurisation reactor 12 via pipes 32 and 36 without any sulphur being removed, the valves 50 and 52 being open.
  • the catalytic partial oxidation reactor 14 is designed to accommodate, or tolerate, some sulphur poisoning of the catalysts.
  • the catalytic partial oxidation reactor 14 is supplied with air from the means 24 to supply air via pipe 26. The air is supplied to the catalytic partial oxidation reactor 14 at an appropriate air to fuel ratio.
  • the catalytic partial oxidation reactor 14 converts the hydrocarbon fuel, natural gas, and air into a gas stream, which contains a high partial pressure of hydrogen and carbon monoxide, e.g. synthesis gas.
  • the gas stream contains hydrogen, water, carbon monoxide, carbon dioxide and nitrogen.
  • the hydrodesulphurisation reactor 12 is supplied with the gas stream, synthesis gas, containing a high partial pressure of hydrogen and carbon monoxide by the catalytic partial oxidation reactor 14 via the pipes 46 and 22 and the recirculating means 54 and this is mixed with the hydrocarbon fuel, natural gas, supplied by the means 20 to supply hydrocarbon fuel.
  • the hydrogen supplied by the catalytic partial oxidation reactor 14 reacts with sulphur compounds present in the hydrocarbon fuel, natural gas, and converts the sulphur compounds into hydrogen sulphide.
  • the hydrogen sulphide is adsorbed onto a bed of zinc oxide in the hydrodesulphurisation reactor 12.
  • the hydrocarbon fuel, natural gas, supplied from the hydrodesulphurisation reactor 12 then contains a very low concentration of sulphur.
  • the supply of hydrocarbon fuel from the desulphurisation reactor 12 to the catalytic partial oxidation reactor 14 and the recirculation of synthesis gas to the desulphurisation reactor 12 from the catalytic partial oxidation reactor 14 occurs during all modes of operation of the fuel processor 10.
  • the combustor 16 is supplied with desulphurised hydrocarbon fuel, natural gas, via pipes 32 and 38 and valve 40. Air is supplied from the means 24 to supply air to the combustor 24 via the pipe 28 and valve 30.
  • the hydrocarbon fuel, natural gas is burned in the air to produce a gas stream depleted of oxygen.
  • the gas stream depleted of oxygen is supplied by the combustor 16 via pipes 42 and 32 to the pre-reformer 18 and at the same time a major portion of the "synthesis gas" is supplied by the catalytic partial oxidation reactor 14 via pipes 44 and 32 to the pre-reformer 18 to mix with the gas stream depleted of oxygen produce a reducing gas mixture that contains approximately 5vol% flammable gases, e.g. "safe gas".
  • the safe gas is supplied from the pre-reformer 18 to the fuel cell arrangement via pipe 48.
  • "safe gas” is supplied to the fuel cell arrangement if the temperature of the solid oxide fuel cell arrangement is higher than 35O 0 C and does not require "synthesis gas” or "processed methane”.
  • a minor portion of the "synthesis gas” is supplied to the desulphurisation reactor 12 via pipes 46 and 22 and the recirculating means 54.
  • the valves 30 and 40 are open, the valve 34 is closed and valves 50 and 52 are open.
  • the desulphurisation reactor 12 increases the supply of desulphurised hydrocarbon fuel, natural gas, to the catalytic partial oxidation reactor 14 via the pipes 32 and 36 and valve 52.
  • the catalytic partial oxidation reactor 14 supplies a major portion of the "synthesis gas" to the pre-reformer 18 via pipes 44 and 32 and a minor portion of the "synthesis gas” to the desulphurisation reactor 12 via pipes 46 and 22 and the recirculating means 54.
  • the valves 30, 34 and 40 are closed.
  • the catalytic partial oxidation reactor 14 supplies the major portion of the "synthesis gas" to the fuel cell arrangement via the pre-former 18 and pipes 44, 32 and 48.
  • a fuel processor is required that provides a fuel supply that is mainly methane and contains as low a concentration of sulphur compounds and higher hydrocarbons as is possible.
  • the hydrodesulphurisation reactor 12 is arranged to supply sufficient desulphurised hydrocarbon fuel, natural gas, to the catalytic partial oxidation reactor 14 via pipes 32 and 36 and the valve 52 such that sufficient hydrogen, "synthesis gas” is produced by the catalytic partial oxidation reactor 12 and supplied to the hydrodesulphurisation reactor 12 via pipes 46 and 22 and the recirculating means 54 to then allow the hydrodesulphurisation reactor 12 to desulphurise the hydrocarbon fuel, natural gas.
  • the remaining "synthesis gas” is supplied by the catalytic partial oxidation reactor 14 to the pre-reformer 18 via pipes 44 and 32.
  • the hydrodesulphurisation reactor 12 supplies desulphurised hydrocarbon fuel to the pre-reformer 18 via the pipe 32 and valve 34.
  • the pre-reformer 18 converts the higher hydrocarbons in the hydrocarbon fuel, natural gas, to methane substantially by hydrogenolysis and the pre- reformer 18 supplies the methane to the fuel cell arrangement via pipe 48.
  • the valves 30 and 40 are closed.
  • the hydrodesulphurisation reactor 12 comprises zinc oxide and copper doped zinc oxide to adsorb the hydrogen sulphide and hydrodesulphurisation catalysts, e.g. nickel molybdate and/or cobalt molybdate.
  • the catalytic partial oxidation reactor 14 comprises partial oxidation catalysts, e.g. one or more of cobalt, nickel, iron, platinum, rhodium, ruthenium or molybdenum.
  • the pre-reformer 18 comprises pre-reforming catalysts, hydrogenolysis catalysts e.g. nickel or cobalt.
  • the advantages of the present invention are that under low load conditions or open circuit conditions of the fuel cell arrangement the fuel processor supplies "synthesis gas" to the fuel cell arrangement and this does not require any further processing by the fuel cell arrangement, e.g. no steam is required.
  • the catalytic partial oxidation reactor provides a controlled desulphurisation process independent of the conditions of the fuel cell arrangement and does not need to follow the load conditions of the fuel cell arrangement.
  • the pre-reformer principally uses hydrogenolysis to convert the higher hydrocarbon fuel to methane.
  • Hydrogenolysis does not require an external supply of water or steam, as does steam reforming, and does not require careful control of the reaction conditions to selectively process higher hydrocarbon fuels and not methane.
  • Hydrogenolysis is ordinarily a reaction in which hydrogen reacts with a hydrocarbon molecule with single bonds between the carbon atoms to break the carbon bond to produce two other lower hydrocarbon molecules.
  • Example 1 propane + hydrogen ethane + methane
  • Example 2 toluene + hydrogen benzene + methane
  • Example 3 butane + hydrogen ethane + ethane.
  • An alternative fuel processor 110 for a fuel cell arrangement comprises a hydrodesulphurisation reactor 12, a catalytic partial oxidation reactor 14, a combustor 16 and a pre-reformer 18.
  • the hydrodesulphurisation reactor 12 is connected to the pre- reformer 18 via a pipe 32 and a valve 34.
  • the catalytic partial oxidation reactor 14 is connected to the means 20 to supply hydrocarbon fuel via a pipe 22A and valve 58.
  • the hydrodesulphurisation reactor 12 is also connected to the combustor 16 via pipes 32 and 38 and a valve 40.
  • the combustor 16 is connected to the pre-reformer 18 via pipe 42.
  • the catalytic partial oxidation reactor 14 is connected to the pre-reformer 18 via pipe 46, the hydrodesulphurisation reactor 12, pipe 32 and valve 34.
  • the catalytic partial oxidation reactor 14 is connected to the hydrodesulphurisation reactor 12 via a pipe 46.
  • the pre-reformer 18 is connected to supply product gases to the fuel cell arrangement, or a further device, via a pipe 48.
  • the fuel processor 110 operates in substantially the same way as described with reference to figure 1. It differs in that the catalytic partial oxidation reactor 14 does not recirculate a portion of the "synthesis gas" to the hydrodesulphurisation reactor 12 rather it supplies all the “synthesis gas” to the hydrodesulphurisation reactor 12. In addition the catalytic partial oxidation reactor 14 is supplied with undesulphurised hydrocarbon fuel, natural gas, and thus the catalytic partial oxidation reactor 14 would have to be tolerant, or more tolerant, to sulphur compounds for the lifetime of the fuel processor 110 or the catalytic partial oxidation processor 14 would have to be replaced at intervals.
  • the fuel processor is applicable to the supply of fuel to a fuel cell arrangements, in particular a solid oxide fuel cell arrangements.
  • the fuel processor may also be suitable for the supply of fuel to other chemical processes .

Abstract

The fuel processor (10) comprises a desulphurisation reactor (12), a catalytic partial oxidation reactor (14), a combustor (16) and a pre-reformer (18), means (20) to supply a hydrocarbon fuel to the desulphurisation reactor (12), means (24) to supply air to the catalytic partial oxidation reactor (14) and means (24) to supply air to the combustor (16) . The desulphurisation reactor (12) is arranged to supply desulphurised hydrocarbon fuel to the catalytic partial oxidation reactor (14) in first, second and third modes of operation, to the combustor (16) in a first mode of operation to the pre-reformer (18) in a third mode of operation. The combustor (16) is arranged to supply oxygen depleted air and steam to the pre-reformer (18) in the first mode of operation. The catalytic partial oxidation reactor (14) is arranged to supply hydrogen to the desulphurisation reactor (12) in all three modes of operation. The catalytic partial oxidation reactor (14) is arranged to supply the pre-reformer (18) in all three modes of operation and the pre-reformer (18) is arranged to supply product gases to the fuel cell arrangement.

Description

A FUEL PROCESSOR FOR A FUEL CELL ARRANGEMENT AND A METHOD OF OPERATING A FUEL PROCESSOR FOR A FUEL CELL ARRANGEMENT
The present invention relates to a fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement.
It is known from European patent EP0673074B1 to provide a fuel cell arrangement comprising a pre-reformer, which is supplied with anode off gas containing hydrogen and steam from the fuel cells and which is supplied with a hydrocarbon fuel. The pre-reformer comprises a catalyst suitable for low temperature steam reforming of the hydrocarbon fuel and a catalyst for partial oxidation reforming of the hydrocarbon fuel. The pre-reformer also comprises a catalyst suitable for hydrodesulphurisation of the hydrocarbon fuel.
A problem with this arrangement is that at low electrical load conditions, or at open circuit conditions, of the fuel cell arrangement, the fuel cells do not generate steam for the low temperature steam reforming reaction. A further problem with this arrangement is that the hydrodesulphurisation of the hydrocarbon fuel is dependent on the rate of anode off gas, hydrogen, recirculation and this is dependent upon the operating conditions of the fuel cell arrangement.
Accordingly the present invention seeks to provide a novel fuel processor for a fuel cell arrangement and a novel method of operating a fuel processor for a fuel cell arrangement to at least reduce or overcome the above- mentioned problem.
Accordingly the present invention provides a fuel processor for a fuel cell arrangement comprising means to supply safe gas to the fuel cell arrangement in a first mode of operation, means to supply synthesis gas to the fuel cell arrangement in a second mode of operation and means to supply processed hydrocarbon fuel to the fuel cell arrangement in a third mode of operation.
Preferably the fuel processor comprises a desulphurisation reactor, a catalytic partial oxidation reactor, a combustor and a pre-reformer, means to supply a hydrocarbon fuel to the desulphurisation reactor, means to supply air to the catalytic partial oxidation reactor, means to supply air to the combustor, the desulphurisation reactor being arranged to supply desulphurised hydrocarbon fuel to the catalytic partial oxidation reactor, the combustor and to the pre-reformer, the combustor being arranged to supply oxygen depleted air and steam to the pre-reformer, the catalytic partial oxidation reactor being arranged to supply hydrogen to the desulphurisation reactor, the catalytic partial oxidation reactor being arranged to supply the pre-reformer, the pre-reformer being arranged to supply product gases to the fuel cell arrangement . Alternatively the fuel processor comprises a desulphurisation reactor, a catalytic partial oxidation reactor, a combustor and a pre-reformer, means to supply a hydrocarbon fuel to the desulphurisation reactor, means to supply hydrocarbon fuel to the catalytic partial oxidation reactor, means to supply air to the catalytic partial oxidation reactor, means to supply air to the combustor, the desulphurisation reactor being arranged to supply desulphurised hydrocarbon fuel to the combustor and to the pre-reformer, the combustor being arranged to supply oxygen depleted air and steam to the pre-reformer, the catalytic partial oxidation reactor being arranged to supply hydrogen to the desulphurisation reactor, the pre-reformer being arranged to supply product gases to the fuel cell arrangement . The present invention also provides a method of operating a fuel processor for a fuel cell arrangement comprising
(a) supplying safe gas to the fuel cell arrangement in a first mode of operation,
(b) supplying synthesis gas to the fuel cell arrangement in a second mode of operation and
(c) supplying processed hydrocarbon fuel to the fuel cell arrangement in a third mode of operation. The first mode is start up and/or shut down conditions of the fuel cell arrangement.
The second mode is hot idle and/or part load conditions of the fuel cell arrangement.
The third mode is normal conditions of the fuel cell arrangement.
The first mode of operation comprises desulphurising a hydrocarbon fuel, carrying out catalytic partial oxidation on the desulphurised hydrocarbon fuel to produce a synthesis gas, burning the desulphurised hydrocarbon fuel to produce oxygen depleted gas and mixing the synthesis gas with the oxygen depleted gas to produce safe gas.
The second mode of operation comprises desulphurising a hydrocarbon fuel, carrying out catalytic partial oxidation on the desulphurised hydrocarbon fuel to produce a synthesis gas.
The third mode of operation comprises desulphurising a hydrocarbon fuel, carrying out catalytic partial oxidation on the desulphurised hydrocarbon fuel to produce a synthesis gas, mixing the synthesis gas with desulphurised hydrocarbon fuel and pre-reforming the desulphurised hydrocarbon fuel to produce the processed hydrocarbon fuel.
The desulphurising comprises mixing synthesis gas and the hydrocarbon fuel to react hydrogen in the synthesis gas with sulphur compounds in the hydrocarbon fuel to form hydrogen sulphide.
The desulphurising comprises adsorbing the hydrogen sulphide. The pre-reforming of the desulphurised hydrocarbon fuel comprises hydrogenolysis .
The safe gas comprises low partial pressures of hydrogen and carbon monoxide. The safe gas contains approximately 5vol% flammable gases and the remainder is non-flammable gases.
The synthesis gas comprises high partial pressures of hydrogen and carbon monoxide. The synthesis gas contains approximately 33 vol% hydrogen and 17 vol% carbon monoxide and the remainder is non-flammable gases. The present invention will be more fully described by way of example with reference to the accompanying drawings in which :-
Figure 1 shows a fuel processor according to the present invention. Figure 2 shows an alternative fuel processor according to the present invention.
A fuel processor 10 for a fuel cell arrangement according to the present invention, as shown in figure 1, comprises a hydrodesulphurisation reactor 12, a catalytic partial oxidation reactor 14, a combustor 16 and a pre- reformer 18. There are means 20 to supply a hydrocarbon fuel to the hydrodesulphurisation reactor 12 via a pipe 22 and there are means 24 to supply air to the catalytic partial oxidation reactor 14 via a pipe 26 and means 24 to supply air to the combustor 16 via a pipe 28 and a valve 30. The hydrodesulphurisation reactor 12 is connected to the pre-reformer 18 via a pipe 32 and a valve 34. The hydrodesulphurisation reactor 12 is connected to the catalytic partial oxidation reactor 14 via pipes 32 and 36. The hydrodesulphurisation reactor 12 is also connected to the combustor 16 via pipes 32 and 38 and a valve 40. The combustor 16 is connected to the pre-reformer 18 via pipes 42 and 32. The catalytic partial oxidation reactor 14 is connected to the pre-reformer 18 via pipes 44 and 32. The catalytic partial oxidation reactor 14 is connected to the hydrodesulphurisation reactor 12 via a pipe 46 and a recirculating means 54, the recirculating means may comprise an ejector, a fan, a pump etc. The pre-reformer 18 is connected to supply product gases to the fuel cell arrangement or, a further device, via a pipe 48.
The means 20 to supply hydrocarbon fuel for example is a supply of natural gas. The means 24 to supply air may be an air compressor, or pump, or an air source within the pressure vessel of the fuel cell arrangement.
In addition a valve 50 may be provided in pipe 26 and a valve 52 may be provided in pipe 36 in order to isolate the catalytic partial oxidation reactor 14 if necessary.
The fuel processor 10 is arranged to perform a number of functions. Firstly the fuel processor 10 is arranged to remove sulphur from the hydrocarbon fuel such that the concentration of sulphur can be tolerated by the catalysts and components of the fuel cells. Secondly the fuel processor 10 is arranged to convert the hydrocarbon into a gas mixture, which contains low partial pressures of hydrogen and carbon monoxide, also known as "safe gas". The "safe gas" contains approximately 5vol% flammable gases and the remainder is non-flammable gases. Thirdly the fuel processor 10 is arranged to convert hydrocarbon fuel into a gas mixture, which contains high partial pressures of hydrogen and carbon monoxide, also known as "synthesis gas or syngas". The "synthesis gas" contains approximately 33 vol% hydrogen and 17 vol% carbon monoxide and the remainder is non-flammable gases. Lastly the fuel processor 10 is arranged to remove higher hydrocarbons, including ethane, ethene, propane, propene, butane, butene, etc by converting them into methane.
The catalytic partial oxidation reactor 14 is arranged to continuously provide hydrogen to the hydrodesulphurisation reactor 12. The catalytic partial oxidation reactor 14 is arranged to provide hydrogen to the pre-reformer 18 during start up of the fuel cell arrangement. During start up of the fuel cell arrangement the hydrogen and carbon monoxide is combined with an excess of non-flammable gases to form the safe gas. The catalytic partial oxidation reactor 14 is also arranged to provide hydrogen and carbon monoxide to the fuel cell arrangement during hot idle conditions and part load conditions of the fuel cell arrangement. During hot idle conditions and part load conditions of the fuel cell arrangement the hydrogen and carbon monoxide is combined with non-flammable gases to form the synthesis gas.
The combustor 16 is arranged to provide oxygen depleted air and steam to the pre-reformer 18 during start up and shut down of the fuel cell arrangement. The combustor 16 may also provide heat to the other reactors during start up such that those reactors reach operational temperature as quickly as possible. The pre-reformer 18 is arranged to provide pre- reforming of higher hydrocarbons, those with more than one carbon atom, to prevent thermal cracking of the higher hydrocarbons in the fuel cell arrangement. The pre- reforming of the higher hydrocarbons is by hydrogenolysis, steam reforming, carbon dioxide reforming, catalytic partial oxidation or any combination of these reactions. The dominant reaction is hydrogenolysis.
In operation hydrocarbon fuel, for example natural gas, is supplied from the means 20 to supply hydrocarbon fuel to the hydrodesulphurisation reactor 12 via pipe 22. Initially the catalytic partial oxidation reactor 14 is supplied with the hydrocarbon fuel, natural gas, from the hydrodesulphurisation reactor 12 via pipes 32 and 36 without any sulphur being removed, the valves 50 and 52 being open. The catalytic partial oxidation reactor 14 is designed to accommodate, or tolerate, some sulphur poisoning of the catalysts. In addition the catalytic partial oxidation reactor 14 is supplied with air from the means 24 to supply air via pipe 26. The air is supplied to the catalytic partial oxidation reactor 14 at an appropriate air to fuel ratio. The catalytic partial oxidation reactor 14 converts the hydrocarbon fuel, natural gas, and air into a gas stream, which contains a high partial pressure of hydrogen and carbon monoxide, e.g. synthesis gas. The gas stream contains hydrogen, water, carbon monoxide, carbon dioxide and nitrogen.
The hydrodesulphurisation reactor 12 is supplied with the gas stream, synthesis gas, containing a high partial pressure of hydrogen and carbon monoxide by the catalytic partial oxidation reactor 14 via the pipes 46 and 22 and the recirculating means 54 and this is mixed with the hydrocarbon fuel, natural gas, supplied by the means 20 to supply hydrocarbon fuel. The hydrogen supplied by the catalytic partial oxidation reactor 14 reacts with sulphur compounds present in the hydrocarbon fuel, natural gas, and converts the sulphur compounds into hydrogen sulphide. The hydrogen sulphide is adsorbed onto a bed of zinc oxide in the hydrodesulphurisation reactor 12. The hydrocarbon fuel, natural gas, supplied from the hydrodesulphurisation reactor 12 then contains a very low concentration of sulphur.
The supply of hydrocarbon fuel from the desulphurisation reactor 12 to the catalytic partial oxidation reactor 14 and the recirculation of synthesis gas to the desulphurisation reactor 12 from the catalytic partial oxidation reactor 14 occurs during all modes of operation of the fuel processor 10. During start up and shut down conditions of the fuel cell arrangement, the combustor 16 is supplied with desulphurised hydrocarbon fuel, natural gas, via pipes 32 and 38 and valve 40. Air is supplied from the means 24 to supply air to the combustor 24 via the pipe 28 and valve 30. The hydrocarbon fuel, natural gas, is burned in the air to produce a gas stream depleted of oxygen. The gas stream depleted of oxygen is supplied by the combustor 16 via pipes 42 and 32 to the pre-reformer 18 and at the same time a major portion of the "synthesis gas" is supplied by the catalytic partial oxidation reactor 14 via pipes 44 and 32 to the pre-reformer 18 to mix with the gas stream depleted of oxygen produce a reducing gas mixture that contains approximately 5vol% flammable gases, e.g. "safe gas". The safe gas is supplied from the pre-reformer 18 to the fuel cell arrangement via pipe 48. "Safe gas" is supplied to the fuel cell arrangement if the temperature of the solid oxide fuel cell arrangement is higher than 35O0C and does not require "synthesis gas" or "processed methane". A minor portion of the "synthesis gas" is supplied to the desulphurisation reactor 12 via pipes 46 and 22 and the recirculating means 54. During this mode of operation the valves 30 and 40 are open, the valve 34 is closed and valves 50 and 52 are open.
During hot idle and part load conditions of the fuel cell arrangement, there is insufficient steam in the recirculated fuel cell anode off gas to perform steam- methane reforming in the reformer in the fuel cell arrangement. A fuel processor is required that does not require steam reforming. During hot idle and part load conditions of the fuel cell arrangement, the desulphurisation reactor 12 increases the supply of desulphurised hydrocarbon fuel, natural gas, to the catalytic partial oxidation reactor 14 via the pipes 32 and 36 and valve 52. The catalytic partial oxidation reactor 14 supplies a major portion of the "synthesis gas" to the pre-reformer 18 via pipes 44 and 32 and a minor portion of the "synthesis gas" to the desulphurisation reactor 12 via pipes 46 and 22 and the recirculating means 54. The valves 30, 34 and 40 are closed. The catalytic partial oxidation reactor 14 supplies the major portion of the "synthesis gas" to the fuel cell arrangement via the pre-former 18 and pipes 44, 32 and 48.
During normal conditions of the fuel cell arrangement, there is sufficient steam in the recirculated fuel cell anode off gas to perform steam-methane reforming in the reformer in the fuel cell arrangement. A fuel processor is required that provides a fuel supply that is mainly methane and contains as low a concentration of sulphur compounds and higher hydrocarbons as is possible. During normal conditions of the fuel cell arrangement, the hydrodesulphurisation reactor 12 is arranged to supply sufficient desulphurised hydrocarbon fuel, natural gas, to the catalytic partial oxidation reactor 14 via pipes 32 and 36 and the valve 52 such that sufficient hydrogen, "synthesis gas" is produced by the catalytic partial oxidation reactor 12 and supplied to the hydrodesulphurisation reactor 12 via pipes 46 and 22 and the recirculating means 54 to then allow the hydrodesulphurisation reactor 12 to desulphurise the hydrocarbon fuel, natural gas. The remaining "synthesis gas" is supplied by the catalytic partial oxidation reactor 14 to the pre-reformer 18 via pipes 44 and 32. In addition the hydrodesulphurisation reactor 12 supplies desulphurised hydrocarbon fuel to the pre-reformer 18 via the pipe 32 and valve 34. The pre-reformer 18 converts the higher hydrocarbons in the hydrocarbon fuel, natural gas, to methane substantially by hydrogenolysis and the pre- reformer 18 supplies the methane to the fuel cell arrangement via pipe 48. The valves 30 and 40 are closed.
The hydrodesulphurisation reactor 12 comprises zinc oxide and copper doped zinc oxide to adsorb the hydrogen sulphide and hydrodesulphurisation catalysts, e.g. nickel molybdate and/or cobalt molybdate.
The catalytic partial oxidation reactor 14 comprises partial oxidation catalysts, e.g. one or more of cobalt, nickel, iron, platinum, rhodium, ruthenium or molybdenum.
The pre-reformer 18 comprises pre-reforming catalysts, hydrogenolysis catalysts e.g. nickel or cobalt.
The advantages of the present invention are that under low load conditions or open circuit conditions of the fuel cell arrangement the fuel processor supplies "synthesis gas" to the fuel cell arrangement and this does not require any further processing by the fuel cell arrangement, e.g. no steam is required. The catalytic partial oxidation reactor provides a controlled desulphurisation process independent of the conditions of the fuel cell arrangement and does not need to follow the load conditions of the fuel cell arrangement.
Further advantages are that the pre-reformer principally uses hydrogenolysis to convert the higher hydrocarbon fuel to methane. Hydrogenolysis does not require an external supply of water or steam, as does steam reforming, and does not require careful control of the reaction conditions to selectively process higher hydrocarbon fuels and not methane.
Additional advantages are that the integration of the hydrodesulphurisation reactor, combustor, partial oxidation reactor and pre-reformer results in a simpler fuel processor process and a reduction in parts. Heat management is easier, the heat produced in one reactor may be used by another reactor. The result is the loss in lower heating value of the hydrocarbon fuel, natural gas, is minimised.
Hydrogenolysis is ordinarily a reaction in which hydrogen reacts with a hydrocarbon molecule with single bonds between the carbon atoms to break the carbon bond to produce two other lower hydrocarbon molecules. Example 1 propane + hydrogen = ethane + methane, Example 2 toluene + hydrogen = benzene + methane, Example 3 butane + hydrogen = ethane + ethane.
An alternative fuel processor 110 for a fuel cell arrangement according to the present invention, as shown in figure 2, comprises a hydrodesulphurisation reactor 12, a catalytic partial oxidation reactor 14, a combustor 16 and a pre-reformer 18. There are means 20 to supply a hydrocarbon fuel to the hydrodesulphurisation reactor 12 via a pipe 22 and valve 56 and there are means 24 to supply air to the catalytic partial oxidation reactor 14 via a pipe 26 and valve 60 and means 24 to supply air to the combustor 16 via a pipe 28 and a valve 30. The hydrodesulphurisation reactor 12 is connected to the pre- reformer 18 via a pipe 32 and a valve 34. The catalytic partial oxidation reactor 14 is connected to the means 20 to supply hydrocarbon fuel via a pipe 22A and valve 58. The hydrodesulphurisation reactor 12 is also connected to the combustor 16 via pipes 32 and 38 and a valve 40. The combustor 16 is connected to the pre-reformer 18 via pipe 42. The catalytic partial oxidation reactor 14 is connected to the pre-reformer 18 via pipe 46, the hydrodesulphurisation reactor 12, pipe 32 and valve 34. The catalytic partial oxidation reactor 14 is connected to the hydrodesulphurisation reactor 12 via a pipe 46. The pre-reformer 18 is connected to supply product gases to the fuel cell arrangement, or a further device, via a pipe 48.
The fuel processor 110 operates in substantially the same way as described with reference to figure 1. It differs in that the catalytic partial oxidation reactor 14 does not recirculate a portion of the "synthesis gas" to the hydrodesulphurisation reactor 12 rather it supplies all the "synthesis gas" to the hydrodesulphurisation reactor 12. In addition the catalytic partial oxidation reactor 14 is supplied with undesulphurised hydrocarbon fuel, natural gas, and thus the catalytic partial oxidation reactor 14 would have to be tolerant, or more tolerant, to sulphur compounds for the lifetime of the fuel processor 110 or the catalytic partial oxidation processor 14 would have to be replaced at intervals.
The fuel processor is applicable to the supply of fuel to a fuel cell arrangements, in particular a solid oxide fuel cell arrangements. However, the fuel processor may also be suitable for the supply of fuel to other chemical processes .

Claims

Claims : -
1. A method of operating a fuel processor for a fuel cell arrangement comprising
(a) supplying safe gas to the fuel cell arrangement in a first mode of operation,
(b) supplying synthesis gas to the fuel cell arrangement in a second mode of operation and
(c) supplying processed hydrocarbon fuel to the fuel cell arrangement in a third mode of operation.
2. A method as claimed in claim 1 wherein the first mode is start up and/or shut down conditions of the fuel cell arrangement .
3. A method as claimed in claim 1 or claim 2 wherein the second mode is hot idle and/or part load conditions of the fuel cell arrangement.
4. A method as claimed in claim 1, claim 2 or claim 3 wherein the third mode is normal conditions of the fuel cell arrangement.
5. A method as claimed in claim 1 wherein the first mode of operation comprises desulphurising a hydrocarbon fuel, carrying out catalytic partial oxidation on the desulphurised hydrocarbon fuel to produce a synthesis gas, burning the desulphurised hydrocarbon fuel to produce oxygen depleted gas and mixing the synthesis gas with the oxygen depleted gas to produce safe gas.
6. A method as claimed in claim 1 wherein the second mode of operation comprises desulphurising a hydrocarbon fuel, carrying out catalytic partial oxidation on the desulphurised hydrocarbon fuel to produce a synthesis gas.
7. A method as claimed in claim 1 wherein the third mode of operation comprises desulphurising a hydrocarbon fuel, carrying out catalytic partial oxidation on the desulphurised hydrocarbon fuel to produce a synthesis gas, mixing the synthesis gas with desulphurised hydrocarbon fuel and pre-reforming the desulphurised hydrocarbon fuel to produce the processed hydrocarbon fuel.
8. A method as claimed in claim 5, claim 6 or claim 7 wherein the desulphurising comprises mixing synthesis gas and the hydrocarbon fuel to react hydrogen in the synthesis gas with sulphur compounds in the hydrocarbon fuel to form hydrogen sulphide.
9. A method as claimed in claim 8 wherein the desulphurising comprises adsorbing the hydrogen sulphide.
10. A method as claimed in claim 7 wherein the pre- reforming of the desulphurised hydrocarbon fuel comprises hydrogenolysis .
11. A fuel processor (10) for a fuel cell arrangement comprising means to supply safe gas to the fuel cell arrangement in a first mode of operation, means to supply synthesis gas to the fuel cell arrangement in a second mode of operation and means to supply processed hydrocarbon fuel to the fuel cell arrangement in a third mode of operation.
12. A fuel processor (10) as claimed in claim 11 comprising a desulphurisation reactor (12), a catalytic partial oxidation reactor (14), a combustor (16) and a pre- reformer (18), means (20) to supply a hydrocarbon fuel to the desulphurisation reactor (12), means (24) to supply air to the catalytic partial oxidation reactor (14), means (24) to supply air to the combustor (16) , the desulphurisation reactor (12) being arranged to supply desulphurised hydrocarbon fuel to the catalytic partial oxidation reactor (14), the combustor (16) and to the pre-reformer (18), the combustor (16) being arranged to supply oxygen depleted air and steam to the pre-reformer (18) , the catalytic partial oxidation reactor (14) being arranged to supply hydrogen to the desulphurisation reactor (12) , the catalytic partial oxidation reactor (14) being arranged to supply hydrogen to the pre-reformer (18), the pre-reformer (18) being arranged to supply product gases to the fuel cell arrangement.
13. A fuel processor (10) as claimed in claim 11 comprising a desulphurisation reactor (12), a catalytic partial oxidation reactor (14), a combustor (16) and a pre- reformer (18), means (20) to supply a hydrocarbon fuel to the desulphurisation reactor (12), means (20) to supply hydrocarbon fuel to the catalytic partial oxidation reactor (14), means (24) to supply air to the catalytic partial oxidation reactor (14), means (24) to supply air to the combustor (16), the desulphurisation reactor (12) being arranged to supply desulphurised hydrocarbon fuel to the combustor (16) and to the pre-reformer (18) , the combustor (16) being arranged to supply oxygen depleted air and steam to the pre-reformer (18) , the catalytic partial oxidation reactor (16) being arranged to supply hydrogen to the desulphurisation reactor (12), the pre-reformer (18) being arranged to supply product gases to the fuel cell arrangement .
14. A fuel processor as claimed in claim 12 or claim 13 wherein the desulphurisation reactor (12) comprises a hydrodesulphurisation catalyst to react hydrogen with sulphur in the hydrocarbon fuel.
15. A fuel processor as claimed in claim 14 wherein the desulphurisation catalyst comprises nickel molydate and/or cobalt molydate.
16. A fuel processor as claimed in any of claims 12 to 15 wherein the desulphurisation reactor (12) comprises zinc oxide and copper doped zinc oxide to absorb hydrogen sulphide.
17. A fuel processor as claimed in any of claims 12 to 16 wherein the pre-former (18) comprises a prereforming catalyst .
18. A fuel processor as claimed in claim 17 wherein the pre-reforming catalyst comprises a hydrogenolysis catalyst.
19. A fuel processor as claimed in claim 17 or claim 18 wherein the catalyst comprises nickel or cobalt.
20. A fuel processor as claimed in any of claims 12 to 19 wherein the catalytic partial oxidation reactor (16) comprises a partial oxidation catalyst.
21. A fuel processor as claimed in claim 20 wherein the partial oxidation catalyst comprises one or more of cobalt, nickel, iron, platinum, rhodium, ruthenium or molymdenum.
PCT/GB2006/000487 2005-03-08 2006-02-13 A fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement WO2006095127A1 (en)

Priority Applications (10)

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EP06709724.6A EP1864350B1 (en) 2005-03-08 2006-02-13 A fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement
AU2006221822A AU2006221822B2 (en) 2005-03-08 2006-02-13 A fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement
JP2008504822A JP5063584B2 (en) 2005-03-08 2006-02-13 FUEL CELL DEVICE FOR FUEL CELL DEVICE AND METHOD OF OPERATING FUEL PROCESSING DEVICE FOR FUEL CELL DEVICE
US11/884,229 US8147571B2 (en) 2005-03-08 2006-02-13 Fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement
KR1020077019109A KR101363337B1 (en) 2005-03-08 2006-02-13 A fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement
DK06709724.6T DK1864350T3 (en) 2005-03-08 2006-02-13 A fuel processor for a fuel cell assembly and a method for operating a fuel processor for a fuel cell assembly
ES06709724.6T ES2476997T3 (en) 2005-03-08 2006-02-13 A fuel processor for a fuel cell configuration and a method for operating a fuel processor for a fuel cell configuration
CA002596919A CA2596919A1 (en) 2005-03-08 2006-02-13 A fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement
US13/292,847 US8470482B2 (en) 2005-03-08 2011-11-09 Fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement
US13/872,710 US8568494B2 (en) 2005-03-08 2013-04-29 Fuel processor for a fuel cell arrangement

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US13/292,847 Division US8470482B2 (en) 2005-03-08 2011-11-09 Fuel processor for a fuel cell arrangement and a method of operating a fuel processor for a fuel cell arrangement

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EP2172421A1 (en) * 2008-04-24 2010-04-07 Panasonic Corporation Hydrogen production device, and fuel cell system provided with the same
EP2799395A1 (en) * 2013-04-30 2014-11-05 Linde Aktiengesellschaft Method for operating a steam reformer and steam reformer
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